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Protein Coding Gene : Med13l mediator complex subunit 13-like
Primary Identifier  MGI:2670178 Organism  mouse, laboratory
Chromosome  5 NCBI Gene Number  76199
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable transcription coregulator activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to act upstream of or within transcription by RNA polymerase II. Part of mediator complex. Is expressed in 1-cell stage embryo; 2-cell stage embryo; cortical plate; and primary oocyte. Human ortholog(s) of this gene implicated in dextro-looped transposition of the great arteries. Orthologous to human MED13L (mediator complex subunit 13L).
  • synonyms:
  • RIKEN cDNA 2210413I17 gene,
  • Med13l,
  • MGI:1922081,
  • 6330591G05Rik,
  • RIKEN cDNA 9030618F05 gene,
  • Thrap2,
  • 9030618F05Rik,
  • mediator complex subunit 13-like,
  • thyroid hormone receptor associated protein 2,
  • MGI:1918805,
  • RIKEN cDNA 6330591G05 gene,
  • Trap240L,
  • 2210413I17Rik,
  • mKIAA1025,
  • MGI:1923449
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Features --> Cross References

Genome

Sequence Feature Displayer

JG Browse Displayer

0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

2 Involved In Mutations

Trail: ProteinCodingGene

0 Strain

0 Transcripts

0 Transgenic Expressors

0 UTRs

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

0 Pathways

0 Targeted By

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

Other

0 Driver For





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